Transgenic Mice Expressing Green Fluorescent Protein under the Control of the Melanocortin-4 Receptor Promoter
Por um escritor misterioso
Descrição
The melanocortin-4 receptor (MC4-R) is an important regulator of energy homeostasis, and evidence suggests that MC4-R-expressing neurons are downstream targets of leptin action. MC4-Rs are broadly expressed in the CNS, and the distribution of MC4-R mRNA has been analyzed most extensively in the rat. However, relatively little is known concerning chemical profiles of MC4-R-expressing neurons. The extent to which central melanocortins act presynaptically or postsynaptically on MC4-Rs is also unknown. To address these issues, we have generated a transgenic mouse line expressing green fluorescent protein (GFP) under the control of the MC4-R promoter, using a modified bacterial artificial chromosome. We have confirmed that the CNS distribution of GFP-producing cells is identical to that of MC4-R mRNA in wild-type mice and that nearly all GFP-producing cells coexpress MC4-R mRNA. For example, cells coexpressing GFP and MC4-R mRNA were distributed in the paraventricular hypothalamic nucleus (PVH) and the dorsal motor nucleus of the vagus (DMV). MC4-R promotor-driven GFP expression was found in PVH cells producing thyrotropin-releasing hormone and in cholinergic DMV cells. Finally, we have observed that a synthetic MC3/4-R agonist, MT-II, depolarizes some GFP-expressing cells, suggesting that MC4-Rs function postsynaptically in some instances and may function presynaptically in others. These studies extend our knowledge of the distribution and function of the MC4-R. The transgenic mouse line should be useful for future studies on the role of melanocortin signaling in regulating feeding behavior and autonomic homeostasis.
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Loss of the melanocortin-4 receptor in mice causes dilated
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Divergence of Melanocortin Pathways in the Control of Food Intake
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Agouti-Related Peptide and MC3/4 Receptor Agonists Both Inhibit
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AgRP neuronal expression of GFP directed by 1-kb AgRP promoter in
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Loss of the melanocortin-4 receptor in mice causes dilated
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IJMS, Free Full-Text
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Collateralizing ventral subiculum melanocortin 4 receptor circuits
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Activation of the Melanocortin-4 receptor signaling by α-MSH
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Transgenic mice with green fluorescent protein-labeled pancreatic
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Loss of the melanocortin-4 receptor in mice causes dilated
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Hypothalamic MC4R regulates glucose homeostasis through adrenaline
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Frontiers Fluorescent transgenic mouse models for whole-brain
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The stimulatory G protein Gsα is required in melanocortin 4
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Reduction of green fluorescent protein (GFP) expression and
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